Daniel, what is the lowest level of manufactured drug quality required to run a phase1 drug trial in Australia?
Is what RAC is producing for RC220 suitable for running US-based phase 3 trials and maybe even being suitable for sale in the US after FDA approval?
could RAC have started these two proposed early-stage clinical trials by using a form of 220 that was faster to produce rather than having to wait till mid year 2024?
Ann: Updated Strategy and Investor Presentation, page-53
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